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Results 1 - 10 of 12 for Familial syndrome associated with hypertrophic cardiomyopathy
  1. SCN5A gene 
    ... SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 5; SCN5A CARDIOMYOPATHY, DILATED, 1E; CMD1E SUDDEN INFANT DEATH SYNDROME VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1 ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10 NCBI ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  2. PRKAG2 gene 
    ... rhythms (arrhythmias) in people with Wolff-Parkinson-White syndrome. More About This Health Condition ... More About This Health Condition Several mutations in ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  3. FKTN gene 
    ... This Health Condition MedlinePlus Genetics provides ... gene can also cause Walker-Warburg syndrome, a severe form of congenital muscular dystrophy that ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  4. MYH6 gene 
    ... This Health Condition MedlinePlus Genetics provides ... atria). Most of the MYH6 gene mutations associated with ASD affect a part of the α- ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  5. MT-TK gene 
    ... C(8356) mitochondrial DNA mutation in a Japanese family. J Neurol. 1996 ... and hearing loss associated with a novel mutation in the mitochondrial tRNA( ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  6. DSP gene 
    ... accounts for the more severe signs and symptoms associated with this condition. ... VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8 EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA CARDIOMYOPATHY, ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  7. CAV3 gene 
    ... Monaco M, Servidei S. Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene. Neuromuscul ... 3 induces persistent late sodium current and is associated with long-QT syndrome. Circulation. 2006 Nov 14;114(20):2104-12. ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  8. LMNA gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  9. MT-TV gene 
    ... novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS. Ital Heart J. 2004 Jun;5(6):460-5. Citation on PubMed Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. MELAS associated with a mutation in the valine transfer RNA ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  10. MT-TH gene 
    ... double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. J Hum Genet. 2003;48(1):47-50. ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
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